1,2,3,4-di-O-sulfanyl-meso-erythritol | 292082-37-2

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机硫酸及其衍生物
• 英文名称: 1,2,3,4-di-O-sulfanyl-meso-erythritol
• 英文别名: (4S)-4-[(4R)-2,2-dioxo-1,3,2-dioxathiolan-4-yl]-1,3,2-dioxathiolane 2,2-dioxide
• CAS: 292082-37-2
• 化学式: C₄H₆O₈S₂
• 分子量: 246.219
• InChiKey: CICIPYWTONFUIR-ZXZARUISSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.2
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  122
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  1,2,3,4-di-O-sulfanyl-meso-erythritol 在 sodium sulfide 作用下， 生成
  参考文献：
  名称：

  Heterocyclisation of free or partially protected alditols via their bis-cyclic sulfate derivatives. Versatile synthesis of aza and thiodeoxyanhydroalditol with erythro, threo, arabino, gulo, talo or manno configuration

  摘要：

  The bis-cyclic sulfate derivatives of erythritol (1), D,L-threitol (5), 3,4-di-O-benzyl-D-mannitol (9), 1,2-O-isopropylidene-D-mannitol (14) and 1-O-benzyl-D,L-xylitol (18) were submitted to nucleophilic attack by allylamine or sodium sulfide. In both cases, heterocyclisation occurred and aza or thioanhydrodeoxyalditols were obtained in moderate to good yields (40 to 89%). With compound 9, 1,5-anhydro-5-thio-L-gulitol (12) was obtained as the main product, a result that is in contrast with previous results reported in the literature using bis-epoxide as bielectrophile intermediate.(1) (C) 2000 Published by Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4039(00)00791-7
• 作为产物：
  描述：

  1,2:3,4-di-O-sulfinyl erythritol 在 ruthenium trichloride 、 sodium periodate 作用下， 以 水 、 异丙醇 、 乙腈 为溶剂， 反应 4.0h， 以26%的产率得到1,2,3,4-di-O-sulfanyl-meso-erythritol
  参考文献：
  名称：

  CYCLIC SULFATE COMPOUND, NON-AQUEOUS ELECTROLYTE SOLUTION CONTAINING SAME, AND LITHIUM SECONDARY BATTERY

  摘要：

  提供一种含有由式(I)表示的环状硫酸酯化合物的非水电解质溶液，其中在式(I)中，R1表示由式(II)表示的基团或由式(III)表示的基团; R2表示氢原子、具有1至6个碳原子的烷基基团、由式(II)表示的基团或由式(III)表示的基团; 在式(II)中，R3表示卤素原子、具有1至6个碳原子的烷基基团、具有1至6个碳原子的卤代烷基基团、具有1至6个碳原子的烷氧基团或由式(IV)表示的基团。

  公开号：

  US20130171514A1

文献信息

• CYCLIC SULFATE COMPOUND, NON-AQUEOUS ELECTROLYTE SOLUTION CONTAINING SAME, AND LITHIUM SECONDARY BATTERY
  申请人：Mio Shigeru

  公开号：US20130171514A1

  公开（公告）日：2013-07-04

  A non-aqueous electrolyte solution containing a cyclic sulfate compound represented by formula (I) is provided, wherein in formula (I), R 1 represents a group represented by formula (II) or a group represented by formula (III); R 2 represents a hydrogen atom, an alkyl group having from 1 to 6 carbon atoms, a group represented by formula (II), or a group represented by formula (III); and in formula (II), R 3 represents a halogen atom, an alkyl group having from 1 to 6 carbon atoms, a halogenated alkyl group having from 1 to 6 carbon atoms, an alkoxy group having from 1 to 6 carbon atoms, or a group represented by formula (IV).

  提供一种含有由式(I)表示的环状硫酸酯化合物的非水电解质溶液，其中在式(I)中，R1表示由式(II)表示的基团或由式(III)表示的基团; R2表示氢原子、具有1至6个碳原子的烷基基团、由式(II)表示的基团或由式(III)表示的基团; 在式(II)中，R3表示卤素原子、具有1至6个碳原子的烷基基团、具有1至6个碳原子的卤代烷基基团、具有1至6个碳原子的烷氧基团或由式(IV)表示的基团。
• Heterocyclisation of free or partially protected alditols via their bis-cyclic sulfate derivatives. Versatile synthesis of aza and thiodeoxyanhydroalditol with erythro, threo, arabino, gulo, talo or manno configuration
  作者：Virginie Glaçon、Mohammed Benazza、Daniel Beaupère、Gilles Demailly

  DOI：10.1016/s0040-4039(00)00791-7

  日期：2000.6

  The bis-cyclic sulfate derivatives of erythritol (1), D,L-threitol (5), 3,4-di-O-benzyl-D-mannitol (9), 1,2-O-isopropylidene-D-mannitol (14) and 1-O-benzyl-D,L-xylitol (18) were submitted to nucleophilic attack by allylamine or sodium sulfide. In both cases, heterocyclisation occurred and aza or thioanhydrodeoxyalditols were obtained in moderate to good yields (40 to 89%). With compound 9, 1,5-anhydro-5-thio-L-gulitol (12) was obtained as the main product, a result that is in contrast with previous results reported in the literature using bis-epoxide as bielectrophile intermediate.(1) (C) 2000 Published by Elsevier Science Ltd.